HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672488Generated: November 1, 2026
4-Methoxyphenylacetic Acid → N-(6-methoxyisoquinolin-3-yl)-2-(4-methoxyphenyl)acetamide
https://huagongshe.com/reaction/1672488
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxyphenylacetic Acid | HCID 7690 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 6-Methoxyisoquinolin-3-amine | HCID 23321157 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(6-methoxyisoquinolin-3-yl)-2-(4-methoxyphenyl)acetamide | HCID 58082419 | 27.3% |
Reaction Steps
To a solution of (4-methoxyphenyl)acetic acid (166.2 mg, 0.86 mmol) in 5 ml of anhydrous THF were added oxalyl chloride (126.9 mg, 4.3 mmol) and 100 ul of DMF. A vigorous effervescence occurred. Within 1-4 minutes the effervescence stopped and the mixture was stirred for 30 minutes at room temperature. Then the 6-methoxyisoquinolin-3-amine (150.0 mg, 0.86 mmol) and Et3N (0.86 mmol) were added. The reaction was stirred at the ambient temperature over 16 hours. The reaction was monitored by LC/MS that showed no more start material left. The reaction crude was purified by a silica gel column to give product 75.7 mg (yield 27.3%). 1H NMR (400 MHz, DMSO-d6) ppm 3.68 (s, 2H), 3.72 (s, 3H), 3.89 (s, 3H), 6.89 (d, J=8.81 Hz, 2H), 7.14 (dd, J=8.94, 2.39 Hz, 1H), 7.26 (d, J=2.27 Hz, 1H), 7.30 (d, J=8.81 Hz, 2H), 7.95 (d, J=9.06 Hz, 1H), 8.32 (s, 1H), 8.98 (s, 1H), 10.73 (s, 1H). HRMS: m/z 323.13882 [M+H]+), calc. 323.13902. MS m/z, (APCI); 323.2 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998978B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-0eedebc388d54154bb1f71413338b6b5 |
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| Source note | uspto-grants-2011_08 |
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